Sutro Biopharma has initiated and is currently enrolling participants for its global Phase 2 trial, REFRαME-L1, which tests luveltamab tazevibulin (luvelta) in NSCLC patients with Folate Receptor-α expression.
Monopar Therapeutics revealed that it has obtained Human Research Ethics Committee (HREC) approval in Australia to initiate a Phase 1 clinical trial for its innovative radiopharmaceutical MNPR-101-Lu.
D&D Pharmatech begins Phase 2 trial for DD01, a long-lasting dual GLP-1/Glucagon receptor agonist, to assess its safety and efficacy in overweight/obese individuals with MASLD/MASH.
Aug 23rd latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.
The U.S. has approved RYBREVANT® (amivantamab-vmjw) and LAZCLUZE™ (lazertinib) as an initial treatment without chemotherapy for patients with advanced lung cancer and EGFR mutations.